# FDA Inspection 1259331 - Remedy Medical Manufacturing - December 12, 2024

Source: https://www.keypedia.com/records/fda_inspections/remedy-medical-manufacturing/798ae375-bde1-49cd-b6e5-930e70ba180e
Source feed: FDA_Inspections

> FDA Inspection 1259331 for Remedy Medical Manufacturing on December 12, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259331
- Company Name: Remedy Medical Manufacturing
- Inspection Date: 2024-12-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1259331 - 2024-12-12](https://www.keypedia.com/records/fda_inspections/remedy-medical-manufacturing/6e5b5001-3b38-4fbb-ac88-980a8a6cf08e)
- [FDA Inspection 1259331 - 2024-12-12](https://www.keypedia.com/records/fda_inspections/remedy-medical-manufacturing/716fd81d-91f5-407c-9529-e4dc7212545f)

Company: https://www.keypedia.com/companies/remedy-medical-manufacturing/735d38a1-5c7b-4926-b8cd-a8a3b879b941

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7